Sexual Differentiation Flashcards

1
Q

Gonadal Ridge

A

Thickened area on the ventromedial surface of the mesonephros

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2
Q

PGCs

A

Migrate to the gonadal ridge via the dorsal mesentary of the hindgut and are rapidly surrounded by cords of somatic cells

*Sex chromosomes of the somatic cells dictate the differentiation of the gonad

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3
Q

First discernible event of testis differentiation

A

Presence of Sertoli cells; aggregate around PGCs to form the testis cords

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4
Q

Appearance of Leydig cells

A

Week 8-9; appear in b/w the developing seminiferous tubules

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5
Q

Primitive Sex cords

A

Extend deep into the medulla of the developing gonads and make contact w/ the epithelium that eventually becomes the tunica albuginea

=>Secondary cords and seminiferous tubules later develop (hardened until puberty)

*Sertoli cells promote this by secreting paracrine factors as well as Leydig proliferation, peritubular myloid cells, and endothelial cells for male vasculature

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6
Q

Requirements for Ovary differentiation (3)

A
  1. Invasion of the cortex (not medulla) by PGCs
  2. Reactivation of the inactivated X-chromosome
  3. Absence of a Y-chromosome
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7
Q

Ovarian Genesis

A

Large pool of oogonia is formed at Week 11 and some leave the pool and enter meiosis until Prophase I

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8
Q

Primordial follicles

A

Formed at Week 13 when granulosa cells aggregate around the oocyte and are covered by a basal lamina

  • By Week 20, oogonial mitosis begins to decline and development of follicles decreases
  • Infant will have all the primordial follicles it will ever have by 6 months old
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9
Q

Male Genital Tract Differentiation

A

Degradation of the Mullerian ducts from Week 7-10 (mediated by AMH)
-released by Sertoli cells

AND

Proliferation of the Wolffian ducts (mediated by testosterone)
=>Vas deferens, epididymis, seminal vesical, prostate

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10
Q

Female Genital Tract Differentiation

A

Persistence of the Mullerian Ducts

AND

Degradation of the Wolffian Ducts

*Occurs in the lack of hormone stimulation

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11
Q

Syndrome of persistent Mullerian Ducts

A

Normal phenotypic male does not produce AMH and has poorly developed female internal genitalia

*Often present in an inguinal hernia

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12
Q

Male External Genitalia Differentiation

A

Occurs w/ the presence of dihydrotestosterone formed from the action of 5a-reductase

*Female external genitalia forms in absence of this

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13
Q

Differentiation of the urogenital sinus

A

Males => Prostatic Buds

Females => Inferior walls of the vagina

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14
Q

Syndrome of Complete Androgen Resistance

A

Male and female internal genitalia is absent; external genitalia is female

-AMH still being secreted means loss of Mullerian; no testosterone means loss of Wolffian

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15
Q

5a-reductase deficiency

A

Internal genitalia will be male; external will be ambiguous

*External may develop more @ puberty

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16
Q

SRY Deficiency

A

Will be a phenotypic female due to lack of SOX 9 and Sertoli cell production

17
Q

47 XXY

A

Klinefelter’s Syndrome: Pts. will be tall (no closure of epiphyseal plates) and have hypogonadism w/ hyalinized tubules

Symptoms include: Gynecomastia
Tall
High-pitched voice
Increased GnRH, FSH, and LH
Increased E2

18
Q

SOX9

A

Encoded by the SRY gene on the Y chromosome; regulates the expression of products that promote Sertoli cell differentiation

19
Q

Genital tubercle

A

Becomes the glans penis or clitoris

20
Q

Genital swelling

A

Becomes the scrotum or the labia majora

21
Q

Genital folds

A

Become the ventral penile folds or the labia minora

22
Q

Barr bodies

A

Inactive X chromosome; males should have none

-Genes in pseudo autosomal region escape inactivation

23
Q

Cortical cords

A

Second wave of cord formation in an XX embryo that eventually break into distinct clusters that are..

=>primordial follicle

24
Q

INSL-3

A

Promotes testicular descent along w/ testosterone

-Also made in the Leydig cells

25
Q

Loss of Intracellular bridges

A

Occurs when spermatozoa are released into the lumen of the seminiferous tubule